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Compound Detail

CHEMBL243676

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O=c1c(O)c(-c2ccc(O)cc2)oc2ccc(O)cc12

Basic Information

ChEMBL ID CHEMBL243676
Phase Preclinical
Structure Type MOL
InChI Key QUPHEKFURGDWME-UHFFFAOYSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
14
Publications
0
Known Names

Molecular Properties

270.2
MW (Da)
2.58
ALogP
5
HBA
3
HBD
90.9
PSA (Ų)
0.63
QED
0
Ro5 Violations
1
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C15H10O5
MW 270.24
Aromatic Rings 3
Heavy Atoms 20
NP-Likeness 0.99

Activity Summary

EC50 1 meas. best 5.63

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Trypanosoma brucei brucei
CHEMBL612851
EC50 5.63 5.63 2320.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
27411733 10.1021/acs.jmedchem.6b00698 Unchecked 4
27411733 10.1021/acs.jmedchem.6b00698 Trypanosoma brucei brucei 3
17166721 10.1016/j.bmc.2006.11.037 Radical scavenging activity 2
19595597 10.1016/j.bmc.2009.06.059 Staphylococcus aureus 2
19595597 10.1016/j.bmc.2009.06.059 Enterococcus faecalis 2
19595597 10.1016/j.bmc.2009.06.059 3-oxoacyl-[acyl-carrier-protein] synthase 3 1
19595597 10.1016/j.bmc.2009.06.059 Escherichia coli 1
27411733 10.1021/acs.jmedchem.6b00698 Dihydrofolate reductase 1
27411733 10.1021/acs.jmedchem.6b00698 Thymidylate synthase 1
27411733 10.1021/acs.jmedchem.6b00698 786-0 1
27411733 10.1021/acs.jmedchem.6b00698 A549 1
27411733 10.1021/acs.jmedchem.6b00698 WI-38 1
27411733 10.1021/acs.jmedchem.6b00698 THP-1 1
27411733 10.1021/acs.jmedchem.6b00698 Cytochrome P450 1A2 1

Data from ChEMBL 36 via Core Engine